Stereocilin gene variants associated with episodic vertigo: expansion of the DFNB16 phenotype
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/s41431-018-0256-6.pdf
Reference20 articles.
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2. Brantberg K. Familial early-onset progressive vestibulopathy without hearing impairment. Acta Otolaryngol. 2003;123:713–7.
3. Eppsteiner RW, Smith RJ. Genetic disorders of the vestibular system. Curr Opin Otolaryngol Head Neck Surg. 2011;19:397–402.
4. Requena T, Espinosa-Sanchez JM, Lopez-Escamez JA. Genetics of dizziness: cerebellar and vestibular disorders. Curr Opin Neurol. 2014;27:98–104.
5. Frejo L, Giegling I, Teggi R, Lopez-Escamez JA, Rujescu D. Genetics of vestibular disorders: pathophysiological insights. J Neurol. 2016;263(Suppl 1):S45–53.
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1. Characterization of Vestibular Phenotypes in Patients with Genetic Hearing Loss;Journal of Clinical Medicine;2024-03-29
2. Novel Pathogenic Variants in the Gene Encoding Stereocilin (STRC) Causing Non-Syndromic Moderate Hearing Loss in Spanish and Argentinean Subjects;Biomedicines;2023-10-31
3. Vertiges positionnels paroxystiques bénins récidivants chez deux enfants DFNB16 d’une même fratrie : cas clinique CARE;Annales françaises d'Oto-rhino-laryngologie et de Pathologie Cervico-faciale;2023-06
4. Types of Inheritance and Genes Associated with Familial Meniere Disease;Journal of the Association for Research in Otolaryngology;2023-04-06
5. Recurrent Benign Paroxysmal Positional Vertigo in DFNB16 Patients with Biallelic STRC Gene Deletions;Otology & Neurotology;2023-02-10
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